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NCT ID: NCT05896410 Not yet recruiting - Clinical trials for Thumb Osteoarthritis

3D-Printed Hand Orthosis Versus Thermoplastic Orthosis

Start date: June 1, 2023
Phase: N/A
Study type: Interventional

This study will investigate the effectiveness of 3D-printed splints for treating thumb osteoarthritis (CMC OA). These splints are made by Occupational Therapists and Physical Therapists out of low-temperature plastic and formed on the patient's hand. 3D printed splints involve photographing the hand and creating a digital file of the splint. This is then printed and fit on the patient. The goal of this cross-over clinical trial is to compare the effectiveness of 3D-printed splints versus thermoplastic splints for treating thumb osteoarthritis (CMC OA). The main question[s] it aims to answer are: Primary objective: • Evaluate the general useability and possible benefits of splint production by 3D printing in a clinical setting Secondary objectives: - Compare the effectiveness of 3D printed orthosis and the low-temperature plastic fabrication manual method in pain reduction - Compare the effectiveness of 3D printed orthosis and the low-temperature plastic fabrication manual method in improving the function. - Compare the satisfaction of patients with the 3D printed orthosis and low-temperature plastic fabrication manual method. - Compare the length of time needed to fabricate each orthosis - Compare the weight of orthosis Participants will provide with two splints (traditional orthosis and 3D-printed orthoses). Participants will use the first orthosis for three weeks, be given a week for washout, and then cross over to the second orthosis.

NCT ID: NCT03736252 Completed - CMC Clinical Trials

Effectiveness of a Neoprene CMC Joint Orthosis

Carpometacar
Start date: November 1, 2018
Phase:
Study type: Observational

Patients will be gathered via convenience sample from a hand therapy clinic. They will be provided with a neoprene commercially available orthosis free of charge. Baseline pain and function will be assessed using the VAS and Functional Index of Hand Arthropathies. Four weeks later, pain, function, and patient satisfaction with the device will be gathered using the Quebec User Evaluation of Assistive Technology questionnaire.